Momentum Posterior Spinal Fixation System
FDA 510(k) K191932 · Ulrich Medical USA
510(k) numberK191932
Submission
- Device name
- Momentum Posterior Spinal Fixation System
- Applicant
- Ulrich Medical USA
Chesterfield, MO, US - Received
- July 19, 2019
- Decision date
- October 2, 2019
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- NKB – Thoracolumbosacral Pedicle Screw System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3070
- Specialty
- Orthopedic
- Implant
- Yes
Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.
Other 510(k)s with product code NKB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262828 | KHEIRON® Spinal Fixation System, including patient specific K-RODNKB · Special | S.M.A.I.O | 09/04/2026SE |
| K260362 | QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS…NKB · Traditional | MANTIZ Co., Ltd. | 07/24/2026SE |
| K253943 | Tiger 2 SystemNKB · Traditional | Zavation Medical Products, LLC | 07/24/2026SE |
| K261284 | Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemNKB · Traditional | Alphatec Spine, Inc. | 07/14/2026SE |
| K253802 | KHEIRON® Spinal Fixation System, including patient specific K-RODNKB · Special | S.M.A.I.O | 07/01/2026SE |
| K253045 | Socko Vimax Spinal Fixation SystemNKB · Traditional | Socko Medical Co., Ltd. | 06/17/2026SE |
| K251251 | ChanPin Pedicle Screw Spinal SystemNKB · Traditional | Chanpin Medtak Co., Ltd. | 06/09/2026SE |
| K260989 | Varion Thoracolumbar Fixation SystemNKB · Traditional | Kyocera Medical Technologies Inc. (KMTI) | 05/15/2026SE |
| K253739 | SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5…NKB · Traditional | Globus Medical, Inc. | 05/07/2026SE |
| K261130 | AccelFix Spinal Fixation SystemNKB · Special | L&K BIOMED Co., Ltd. | 05/05/2026SE |
More from L&K BIOMED Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K252087 | Navigation Module of the Cortium® SystemOLO · Traditional | 02/03/2026SE |
| K251719 | Momentum® Posterior Spinal Fixation SystemNKB · Special | 07/01/2025SE |
| K241396 | uCerv Flux-C 3D Porous Titanium Cervical InterbodyODP · Special | 05/23/2024SE |
| K240515 | uNion® MAX Cervical Plate SystemKWQ · Special | 03/18/2024SE |
| K231809 | Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS…PML · Traditional | 10/20/2023SE |
| K230614 | CortiumNKG · Traditional | 05/02/2023SE |
| K223274 | Momentum® MIS Posterior Spinal Fixation SystemNKB · Special | 11/28/2022SE |
| K220696 | uCerv Flux-C 3D Porous Titanium Cervical InterbodyODP · Traditional | 08/19/2022SE |
| K200845 | Navigation Module of the Momentum SystemOLO · Traditional | 09/10/2020SE |
| K181921 | Solidity Vertebral Body ReplacementMQP · Traditional | 11/16/2018SE |
Questions and answers
When was Momentum Posterior Spinal Fixation System cleared by the FDA?
Momentum Posterior Spinal Fixation System (K191932) received a 510(k) decision of Substantially Equivalent on October 2, 2019, 75 days after the submission was received.
What is the product code of K191932?
The FDA product code is NKB – Thoracolumbosacral Pedicle Screw System, a Class II (moderate risk) device regulated under 21 CFR 888.3070.